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Cryptic fragment α 4 LG4‐5 derived from laminin α 4 chain inhibits de novo adipogenesis by modulating the effect of fibroblast growth factor‐2
Author(s) -
Yamashita Hironobu,
Goto Chie,
Tajima Rie,
Koparal Ayse Tansu,
Kobori Masato,
Ohki Yuji,
Shitara Kenya,
Narita Ryo,
Toriyama Kazuhiro,
Torii Shuhei,
Niimi Tomoaki,
Kitagawa Yasuo
Publication year - 2008
Publication title -
development, growth and differentiation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 66
eISSN - 1440-169X
pISSN - 0012-1592
DOI - 10.1111/j.1440-169x.2007.00979.x
Subject(s) - adipogenesis , laminin , matrigel , microbiology and biotechnology , biology , extracellular matrix , growth factor , proteolysis , fibroblast growth factor , extracellular , receptor , biochemistry , cell , enzyme , mesenchymal stem cell
Cleavage of the extracellular matrix (ECM) by proteolysis unmasks cryptic sites and generates novel fragments with biological activities functionally distinct from those of the intact ECM molecule. The laminin G‐like (LG)4‐5 fragment has been shown to be excised from the laminin α 4 chain in various tissues. However, the functional role of this fragment has remained unknown to date. To investigate this, we prepared α 4 LG1‐3 and α 4 LG4‐5 fragments by elastase digestion of recombinant α 4 LG1‐5, and examined their effects on de novo adipogenesis in mice at the site of injection of basement membrane extract (Matrigel) and fibroblast growth factor (FGF)‐2. Although the addition of whole α 4 LG1‐5 suppressed adipogenesis to some extent, the α 4 LG4‐5 fragment could strongly suppress adipogenesis at a concentration of less than 20 n m . Addition of the α 4 LG4 module, which contains a heparin‐binding region, had a suppressive effect, but this was lost in mutants with reduced heparin‐binding activity. In addition, antibodies against the extracellular domain of syndecan‐2 and ‐4, which are known receptors for the α 4 LG4 module, suppressed adipogenesis. Thus, these results suggest that the cryptic α 4 LG4‐5 fragment derived from the laminin α 4 chain inhibits de novo adipogenesis by modulating the effect of FGF‐2 through syndecans.